Identification of a Novel Hemizygous SQSTM1 Nonsense Mutation in Atypical Behavioral Variant Frontotemporal Dementia.

about

Identification of a Novel Hemizygous SQSTM1 Nonsense Mutation in Atypical Behavioral Variant Frontotemporal Dementia.

Item

http://www.wikidata.org/entity/Q50234470

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@en

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@nl

type

Item

label

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@en

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@nl

prefLabel

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@en

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@nl

P1476

Identification of a Novel Hemi ...... riant Frontotemporal Dementia.

@en

P2093

Honghua Zheng

http://www.w3.org/2001/XMLSchema#string

Lin Sun

http://www.w3.org/2001/XMLSchema#string

Shifu Xiao

http://www.w3.org/2001/XMLSchema#string

Wei Li

http://www.w3.org/2001/XMLSchema#string

Xia Li

http://www.w3.org/2001/XMLSchema#string

P2860

Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice

Rapidly Progressive Frontotemporal Dementia Associated with MAPT Mutation G389R.

A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation.

Apolipoprotein Ε ε4 frequency is increased among Chinese patients with frontotemporal dementia and Alzheimer's disease

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Human nonsense-mediated mRNA decay factor UPF2 interacts directly with eRF3 and the SURF complex

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.

Diagnostic utility of ASL-MRI and FDG-PET in the behavioral variant of FTD and AD.

P304

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3389/FNAGI.2018.00026

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Zhouyi Rong

P577

2018-02-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29467647

http://www.w3.org/2001/XMLSchema#string

P932

5808128

http://www.w3.org/2001/XMLSchema#string